New study tracks rare childhood brain disorder to pave way for future treatments
NCT ID NCT07531511
First seen Apr 26, 2026 · Last updated May 05, 2026 · Updated 2 times
Summary
This study follows 60 children with SLC6A1-NDD, a rare genetic condition causing seizures and developmental delays. Researchers will track seizures, behavior, and development over time to better understand the disease. The goal is to prepare for future clinical trials by learning which tests work best.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Conditions
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